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Diclofenac Potassium

NDC 51672-4240, Diclofenac Potassium, powder, for solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4240
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4240 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC POTASSIUM50 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
51672-4240-6516724240069 PACKET in 1 CARTON (51672-4240-6) / 1 POWDER, FOR SOLUTION in 1 PACKET (51672-4240-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68a926a2-b818-420f-9c9a-fd91dc5a8f36

  • NADAC price for package 51672424006

    GET /v1/drugs/nadac/51672424006

Use it

Look up 51672-4240 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4240 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4240. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.